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High Temperature Studies with Co2 Laser Heated Sapphire: Reactivity and Surface Structures

Published online by Cambridge University Press:  28 February 2011

Hayim Abrevaya
Affiliation:
Signal Research Center Inc., 50 East Algonquin Road, Box 5016, Des Plaines, IL 60017
Paul C. Nordine
Affiliation:
Midwest Research Institute, 425 Volker Boulevard, Kansas City, MO 64110
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Abstract

CO2 Laser heating of c-axis sapphire filaments was used in a low pressure flow reactor in order to study evaporation and chlorination of single crystal and liquid aluminas. Reacted specimens were examined by scanning electron microscopy (SEM) to monitor the evolution of facets and other surface structures with reaction conditions.

An increase of the incident energy on a laser heated sapphire filament at the melting point does not result in complete melting, because the semi-transparent melt layer that forms has a higher effective emittance than the solid. This technique allows simultaneous reactivity study of liquid and single crystal aluminas at the melting point, as well as study of reactions of single crystal alumina at lower temperatures.

Sapphire specimens develop a hexagonal prism shape after reaction with chlorine containing gases whereas evaporation does not change the initially cylindrical specimen shape.

The primary structural characteristic of the 0.025 cm as-received sapphire specimens from Tyco is the presence of ∼1μm voids that are produced during the growth of the crystal. These voids form conical arrays 20–30μm apart along the filament axis. Specimens reacted with chlorine containing gases below ∼1900K exhibit surface structures which form arrays with the same size and pattern as the voids in the as-received specimens.

Type
Research Article
Copyright
Copyright © Materials Research Society 1986

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References

1. Billard, D. and Piriou, B., Mat. Res. Bull. 9, 943950 (1974).CrossRefGoogle Scholar
2. Abrevaya, H., PhD thesis, Yale University, New Haven (1982).Google Scholar
3. Pollack, J. J. A., J. Mat. Sci., 7, 631648 (1972); 7, 649–653 (1972).CrossRefGoogle Scholar
4. Tyrolerava, J. and Lu, W. K., J. Amer. Ceram. Soc., 52 (2), 7779 (1969).CrossRefGoogle Scholar
5. Cockayne, B., Chesswas, M., and Gasson, D.B., J. Mat. Sci., 2, 711 (1967).CrossRefGoogle Scholar
6. Paule, R. C., High Temp. Science, 8, 257266 (1976).Google Scholar
7. Nelson, L. S., Richardson, N. L., Keil, K. and Skaggs, R., High Temp. Science, 5, 138154 (1973).Google Scholar
8. Gryvnak, D. A. and Burch, D. E., J. Optic. Soc. America, 55 (6), 625630 (1965).CrossRefGoogle Scholar
9. Peleg, M. and Alcock, C. B., High Temp. Science, 6, 5263 (1974).Google Scholar
10. Fu, C. M. and Burns, R. P., High Temp. Science, 8, 257266 (1976).Google Scholar